PlainRecalls

Zimmer, Inc.

297 recalls on record · Latest: Dec 31, 2025

Zimmer, Inc. Recall Insight

Zimmer, Inc. appears on 297 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.354% of the federal archive — a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Dec 31, 2025, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 47 entries, severity tagging shows 0 critical, 47 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 47 of 47 entries — unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (47). The date window on this page runs from Jul 18, 2012 to Nov 28, 2012.

Manufacturer-level browsing is useful when monitoring a single firm for patterns — whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current — deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement — always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Nov 28, 2012

00780302801 MIS 12/14 Slotted Femoral Head Provisional -3.5X28 00780302802 MIS 12/14 Slotted Femoral Head Provisional +0X28 00780302803 MIS 12/14 S…

FDA Devices Moderate Nov 28, 2012

Multipolar¿ Bipolar Cup Liner 22 mm LD.; Item 00-5001-040-22 Product Usage: The liner snaps into the Multipolar¿ Bipolar Cup and serves as the …

FDA Devices Moderate Nov 28, 2012

00780302601 MIS 12/14 Slotted Femoral Head Provisional -3.5X26 00780302602 MIS 12/14 Slotted Femoral Head Provisional +0X26 00780302603 MIS 12/14 S…

FDA Devices Moderate Nov 28, 2012

00789503201 VerSys Femoral Head Provisional 32mm -3.5 00789503202 VerSys Femoral Head Provisional 32mm +0 00789503203 VerSys Femoral Head Provision…

FDA Devices Moderate Nov 14, 2012

Dynesys¿ Top-Loading System Cannulated Pedicle + Set Screw

FDA Devices Moderate Nov 14, 2012

NCB¿ screw ¿ 4.0 self-tapping

FDA Devices Moderate Nov 14, 2012

DTO" Implant

FDA Devices Moderate Nov 14, 2012

Anatomical Shoulder" Fracture Humeral stem

FDA Devices Moderate Nov 14, 2012

Alloclassic SL Shaft

FDA Devices Moderate Nov 14, 2012

Anatomical Shoulder" Inverse/Reverse Humeral PE-Insert Sterile, Rx

FDA Devices Moderate Nov 14, 2012

Biolox¿ Option Ceramic Femoral Head System Rx, sterile

FDA Devices Moderate Nov 14, 2012

zimmer Anatomical Shoulder Glenoid S, cemented, sterile; REF 01.04214.340 PE Keeled Glenoid S, cemented, sterile; REF 01.04214.345, Glenoid M, ce…

FDA Devices Moderate Nov 14, 2012

Anatomical Shoulder" Inverse Humeral Cup

FDA Devices Moderate Nov 14, 2012

Anatomical Shoulder" Inverse/Reverse Glenoid Sterile, Rx

FDA Devices Moderate Nov 14, 2012

Dynesys¿ Revision + set screw

FDA Devices Moderate Nov 14, 2012

MS-30¿ Stem

FDA Devices Moderate Nov 14, 2012

Anatomical Shoulder" Humeral stem

FDA Devices Moderate Nov 14, 2012

MS-30¿ Distal centralizer, cemented, sterile, Rx

FDA Devices Moderate Nov 14, 2012

CLS Stem

FDA Devices Moderate Nov 14, 2012

Original M.E. Mueller" Low Profile Cup Sterile, Rx

FDA Devices Moderate Nov 14, 2012

Anatomical Shoulder" Humeral Head

FDA Devices Moderate Nov 14, 2012

NCB¿ cancellous screw

FDA Devices Moderate Nov 14, 2012

Kopf Adapter S Sterile, Rx

FDA Devices Moderate Nov 14, 2012

Fitmore" Hip Stem

FDA Devices Moderate Nov 14, 2012

Dynesys¿ HA Pedicle + set screw

FDA Devices Moderate Nov 14, 2012

NCB¿-PH Plate

FDA Devices Moderate Nov 14, 2012

Metasul¿ Durom¿ Femoral component Sterile, Rx

FDA Devices Moderate Nov 14, 2012

Dynesys¿ Set screw M6

FDA Devices Moderate Nov 14, 2012

Dynesys¿ Universal spacer 6-45

FDA Devices Moderate Oct 24, 2012

CPT Femoral Stem 12/14 Neck Taper Extended Offset,(item 00-8114-001-10. CPT stems are primary cemented femoral hip stems used by surgeons in total…

FDA Devices Moderate Oct 24, 2012

CPT Modular Stem, Item No. 00-8011-001-00; Lot 61947708. CPT stems are primary cemented femoral hip stems used by surgeons in total hip arthroplas…

FDA Devices Moderate Oct 24, 2012

CPT Hip System Femoral Stem Petite, Item No. 00-8011-000-05. CPT stems are primary cemented femoral hip stems used by surgeons in total hip arthro…

FDA Devices Moderate Oct 10, 2012

00789502202 VerSys Femoral Head Provisional 22mm +0 00789502203 VerSys Femoral Head Provisional 22mm +3.5 00789502220 VerSys Femoral Head Provision…

FDA Devices Moderate Oct 10, 2012

00780303601 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780303602 MIS 12/14 Slotted Femoral Head Provisional +0X36 00780303603 MIS 12/14 S…

FDA Devices Moderate Oct 10, 2012

Cemented Tibial Drill Product Usage: The cemented tibial drill is used to prepare the tibial bone prior to the impaction of the applicable stemme…

FDA Devices Moderate Oct 10, 2012

00780303201 MIS 12/14 Slotted Femoral Head Provisional -3.5X32 00780303202 MIS 12/14 Slotted Femoral Head Provisional +0X32 00780303203 MIS 12/14 S…

FDA Devices Moderate Oct 10, 2012

00780302801 MIS 12/14 Slotted Femoral Head Provisional -3.5X28 00780302802 MIS 12/14 Slotted Femoral Head Provisional +0X28 00780302803 MIS 12/14 S…

FDA Devices Moderate Oct 10, 2012

00780302201 MIS 12/14 Slotted Femoral Head Provisional -2X22 00780302202 MIS 12/14 Slotted Femoral Head Provisional +0X22 00780302203 MIS 12/14 Slo…

FDA Devices Moderate Oct 10, 2012

00789502601 VerSys Femoral Head Provisional 26mm -3.5 00789502602 VerSys Femoral Head Provisional 26mm +0 00789502603 VerSys Femoral Head Provision…

FDA Devices Moderate Oct 10, 2012

12/14 Neck Taper 00789504001 VerSys Femoral Head Provisional 40mm -3.5 00789504002 VerSys Femoral Head Provisional 40mm +0 00789504003 VerSys Femo…

FDA Devices Moderate Aug 22, 2012

00-4309-029-01 - Trabecular Metal Reverse Shoulder Liner 36 mm 65¿¿ Neck Angle Per surgical technique 97-4309-003-00 Revision 4: "Complete Poly Line…

FDA Devices Moderate Aug 22, 2012

Trabecular Metal Reverse Shoulder Liner 40mm, part 00-4309-028-00 - Per surgical technique 97-4309-003-00 Revision 4: "Complete Poly Liner insert…

FDA Devices Moderate Aug 22, 2012

The NCB Polyaxial Locking Plate System NCB screws 26mm: 02.03155.026, non-sterile Product is implantable screws indicated for temporary internal f…

FDA Devices Moderate Aug 8, 2012

Nextgen Complete Knee Solution Femoral and Provisional Impactor/ Extractor, REF 00-5901-026-00, Non-Sterile Zimmer, Warsaw Indiana The instrument…

FDA Devices Moderate Aug 8, 2012

Nextgen Complete Knee Solution Replacement Jaw for Use with Femoral and Provisional Impactor/Extractor, REF 00-5901-026-40, Non-Sterile Zimmer, Warsa…

FDA Devices Moderate Jul 18, 2012

Pathfinder NXT Fixed Percutaneous Rod Holder, Part numbers 3573-2 (straight handle) Stainless Steel / Silicone Rubber, Rx only, non sterile. Produ…

FDA Devices Moderate Jul 18, 2012

Pathfinder NXT Fixed Percutaneous Rod Holder, Part numbers 3573-1 (angle handle) , Stainless Steel / Silicone Rubber, Rx only, non sterile. Produc…

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Data Sources

  • Source: FDA + CPSC + NHTSA + USDA FSIS — federal recall filings naming this firm. Verify with FDA, CPSC, NHTSA, or USDA FSIS directly.
  • Source: PlainRecalls Manufacturer Index — firm-level aggregation across all four federal recall feeds